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U.S. Department of Health and Human Services

Import Refusal Report

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Refusal Actions by FDA as Recorded in OASIS

for 84-Neurological


Entry/doc/line/sfx Refusal Date Product
Code
Manufacturer
FEI
Manufacturer
Name
Manufacturer
Country/Area
310-9703307-5/1/1 16-Sep-2005 84GWM 3005137201 Aremco Grove House United Kingdom
 
DQ4-4781606-6/1/1 23-Sep-2005 84GZJ 3002808181 Skylark Device & Systems Co., Ltd. Taiwan
 
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